ACETYLCHOLINESTERASE INHIBITORY EFFECT OF 3-(1H-INDOL-3-YL)-1, 3-DIPHENYLPROPAN-1-ONE DERIVATIVES

Authors

  • Manjunatha KS Department of Pharmaceutical Chemistry, Kuvempu University, Post Graduate Centre, Kadur - 577 548, Chikkamagalur, Karnataka,India.
  • Manu Cp Department of Pharmaceutical Chemistry, Kuvempu University, Post Graduate Centre, Kadur - 577 548, Chikkamagalur, Karnataka, India.
  • Satyanarayan Nd Department of Pharmaceutical Chemistry, Kuvempu University, Post Graduate Centre, Kadur - 577 548, Chikkamagalur, Karnataka, India.
  • Vinay Kn Department of Chemistry, Tumkur University, Tumkur - 572 101, Karnataka, India
  • Vineetha Ms Department of Biochemistry, Centre for Post Graduate Studies, Jain University, Bengaluru, Karnataka, India.
  • Sunil More S School of Basic and Applied Sciences, Dayananda Sagar University, K.S. Layout, SM Hills, Bengaluru - 560 078, Karnataka, India

DOI:

https://doi.org/10.22159/ajpcr.2017.v10i8.18730

Keywords:

Nil, Neurotransmitter, Dementia, Bovine serum albumin, Nil, Physostigmine

Abstract

Objective: The objective of the study is acetylcholinesterase (AChE) inhibitory effect of 3-(1H-indol-3-yl)-1, 3-diphenylpropan-1-one derivatives by Ellman's method, physostigmine is used as positive control.

Method: 3-(1H-indol-3-yl)-1, 3-diphenylpropan-1-one derivatives were synthesized by the addition of chalcone (0.25 g, 1 mmol), indole (0.12 g, 1 mmol) in ethanol (5 ml), and concentrated hydrochloric acid (5 mmol %). These earlier synthesized compounds were screened for AChE inhibitors by modifying Ellman's method.

Results: Among the tested compounds, 3a and 3j were found to be having more potential than other compounds with half maximal inhibitory concentration values of 13.64 and 14.3 μg/ml, respectively. Whereas, compounds 3c, 3e, 3g, and 3i exhibited an average AChE inhibition of 16.4, 17.9, 17.6, and 21.1 μg/ml, respectively.

Conclusion: The compounds 3-(1H-indol-3-yl)-1, 3-diphenylpropan-1-one derivatives were found to be possible lead molecules in AChE inhibition and even though, the molecules were structurally dissimilar to that of the standard, still they exhibited a considerable degree of inhibition and encourage the researchers to look into the mode of action of their inhibition ability against AChE.

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Published

01-08-2017

How to Cite

KS, M., M. Cp, S. Nd, V. Kn, V. Ms, and S. More S. “ACETYLCHOLINESTERASE INHIBITORY EFFECT OF 3-(1H-INDOL-3-YL)-1, 3-DIPHENYLPROPAN-1-ONE DERIVATIVES”. Asian Journal of Pharmaceutical and Clinical Research, vol. 10, no. 8, Aug. 2017, pp. 83-86, doi:10.22159/ajpcr.2017.v10i8.18730.

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